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CANDELA SCLERO LONG PULSE DYE LASER

Page Type
Cleared 510(K)
510(k) Number
K993671
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/2000
Days to Decision
84 days
Submission Type
Summary

CANDELA SCLERO LONG PULSE DYE LASER

Page Type
Cleared 510(K)
510(k) Number
K993671
510(k) Type
Traditional
Applicant
CANDELA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/2000
Days to Decision
84 days
Submission Type
Summary